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Can special exercises ease chronic back pain? new study aims to find out

NCT ID NCT07475481

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will test different exercise programs for adults aged 40 to 60 with chronic low back pain. Participants will be assigned to gym-based resistance training, physiotherapy exercises, or home-based routines, some with a special belt that gives feedback on core muscle activity. The goal is to see which approach best reduces pain and improves physical function over 8 weeks.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
supervised resistance training and developmental position-based exercise, with or without real-time intra-abdominal pressure biofeedback
What this could lead to
If successful, this could point toward effective exercise strategies to reduce pain and improve function in people with chronic low back pain.
What could go wrong
This is a small, early-stage trial (120 participants) that has not yet started recruiting. Results may not apply to all back pain sufferers, and exercise programs require ongoing commitment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 120 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2027

An estimate. Start dates often move.

Expected to finish

Mar 2030

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

40 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Chronic low back pain lasting more than 12 weeks, with current low back pain at screening/baseline. * Resting blood pressure below 139/89 mmHg. * Health status allowing participation in moderate-intensity resistance training and aerobic activity. * Physically active, but not professional athletes. * Non-smoker. * Able and willing to provide written informed consent and comply with study procedures Exclusion Criteria: * Absolute or relative contraindications to resistance training or other clinically relevant cardiovascular contraindications. * Coronary artery disease, heart rhythm disorders, acute myocarditis, Marfan syndrome, or other cardiovascular conditions judged unsafe by the study physician. * History of myocardial infarction, cerebrovascular disease, peripheral vascular disease, or grade II-IV hypertension. * Type 1 or type 2 diabetes mellitus. * Severe obesity (BMI \>= 40.0 kg/m2). * Infectious disease at screening (for example, COVID-19 or influenza). * Current treatment for chronic low back pain from another healthcare provider. * Prior spine surgery or lower-limb surgery. * Structural spinal deformity such as spondylolisthesis or spondylolysis. * Spinal fracture, inflammatory spinal disorder, or neurological signs of nerve root compromise, including decreased tendon reflexes, sensory loss, or motor deficits. * Dizziness during exercise. * Use of medications other than analgesics and non-steroidal anti-inflammatory drugs, unless specifically approved by the study physician.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Faculty of Physical Education and Sport, Chrales University

    Prague, 162 52, Czechia

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